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Hydrocarbons pentane

Rigid polyurethane foams used in refrigerators and freezers - Alternatives include hydrocarbons (pentane) and HCFC-141b long-term alternatives include HFCs (134a, -245, -356, -365). Vacuum panels may be used in the future. [Pg.34]

The blowing agent can be a hydrocarbon (pentane, for example), which is easily flammable, and precautions against fire must be taken at all the stages of transport, handling, storage, manufacture... [Pg.741]

Soluble in alcohol, ether (Weast, 1986), and many low molecular weight hydrocarbons (pentane, hexane, heptane), and halogenated hydrocarbons such as chloroform, methylene chloride, trichloroethylene. [Pg.301]

Bridie et al. [27] have studied the solvent extraction of hydrocarbons and their oxidative products from oxidised and non-oxidised kerosine-water mixtures, using pentane, chloroform and carbon tetrachloride. Extracts are treated with Florasil to remove non-hydrocarbons before analysis by temperature programmed gas chromatography. From the results reported it is concluded that, although each of the solvents extracts the same amount of hydrocarbons, pentane extracts the smallest amount of non hydrocarbons. Florasil effectively removes non hydrocarbons from pentane extracts, but also removes 10-25% of aromatic hydrocarbons. However, as the other solvents are less susceptible than pentane to treatment with Florasil, pentane is considered by those workers to be the most suitable solvent for use in determining oil in water. [Pg.255]

To prevent the inverse flow of the product, backflow gates should be used. Workshops for organoaluminum compounds should not be fitted with water and vapour piping. Heat carriers can be only inert hydrocarbons (pentane, mineral oil, etc.). Tanks and reactors should have drains. Dirt can be separated with highly productive hermeticised centrifuges. [Pg.387]

This name is derived from the five carbon hydrocarbon, pentane.)... [Pg.482]

Natural gas is a naturally occurring mixture of simple hydrocarbons and nonhydrocarbons that exists as a gas at ordinary pressures and temperatures. In the raw state, as produced from the earth, natural gas consists principally of methane (CH4) and ethane (C2H4), with fractional amounts of propane (C3H8), butane (C4H,0), and other hydrocarbons, pentane (C5H,2) and heavier. Occasionally, small traces of light aromatic hydrocarbons such as benzene and toluene may also be present. [Pg.907]

There are three different structures for the hydrocarbon pentane, C5H12. These structures are called geometric isomers because each has a different shape. Draw electron dot diagrams for the three possibilities. You can substitute a dash, like the stick in the gmndrop models, to represent each pair of electrons. [Pg.337]

In the free state the compounds decompose at once into dialkyl aluminum halide and hydrocarbon (mainly ethylene with a little cyclopropane). But at very low temperatures ( —80°C) it is possible to isolate, for example, iodomethyldiethylalane in hydrocarbon (pentane) solution 97, 98). [Pg.277]

Boraadamantanes are readily soluble in chlorinated hydrocarbons (chloroform, methylene chloride, carbon tetrachloride) and in benzene. The parent 1-boraadamantane (5) can be recrystallized from hydrocarbons (pentane), whereas alkyl derivatives are soluble in these solvents. More polar solvents either react or give complexes with 1-boraadamantanes. [Pg.905]

The hydrocarbon, pentane, fails to produce the oxonium salt,... [Pg.597]

Use of FCHCs as blowing agents and refrigerants has been prohibited since the mid-1990s due to long-term damage done to the ozone layer protecting the earth. The substances now used instead are the less harmful HF(C)CH and/or the hydrocarbons (pentane, cyclopentane). [Pg.125]

Diethyl ether, acetone and low molecular weight hydrocarbons, pentane or hexane, are commonly employed. Ether and acetone is more advantage due to its better ability to dissolve more oxygenated compounds. The advantage of these solvents are their high volatility, 34.6°C, 56°C for ether and acetone and 36°C and 54°C for pentane and hexane, respectively. The tendency of these solvents interfering the elution of the peaks of the volatile components is low. Further more if the extract has to be concentrated, these solvents are easily expelled. [Pg.273]

What mass of carbon dioxide is produced by the complete combustion of 100. g of the hydrocarbon pentane, C5H12 ... [Pg.176]

Since the gel permeation method does not allow a direct determination of the molecular weights or molar volumes of the samples under investigation, calibrations are made by using standard compoimds in the form of a graphic dependence of their molar volume on the elution volume. Normal hydrocarbons (pentane, hexane, heptane, dodecane, hexadecane, octadecane) and aliphatic esters (octyl adipate and octyl sebacate) are used as standards. The molar volumes (ml/mole) were plotted against elution volumes, V (ml) in the calibration curves, as shown in Table 7.19. The molar volumes were calculated from the atomic volumes and structural coefScients. ... [Pg.270]

As shown in Table 12.2, a solution always forms if the solvent-solute interactions are comparable to, or stronger than, the solvent-solvent interactions and the solute-solute interactions. For example, consider mixing the hydrocarbons pentane (C5Hj2) and heptane (C7H15). The intennolecular forces present within both pentane and heptane are dispersion forces. Similarly, the intennolecular forces present between heptane and pentane are also dispersion forces. All three interactions are of similar magnitude so the two substances are soluble in each other in all proportions—they are said to be miscible. The formation of the solution is driven by the tendency toward mixing, or toward greater entropy, that we just discussed. [Pg.549]

The mass spectra of the isomeric hydrocarbons pentane, 2-methylbutane, and 2,2-dimethylpropane (Figures 11-25, 11-26, and 11-27) reveal the relative ease of the several possible C-C bond-dissociation processes. In each case, the molecular ion produces a relatively weak peak otherwise, the spectra of the three compounds are very different. [Pg.465]


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See also in sourсe #XX -- [ Pg.504 ]




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Pentane-extractable hydrocarbons

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